@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP266371.RArVw0uBDN5d2R_vqkSbGXqej4X2G7fGrGZ5ZEJAfdBgE> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP266371.RArVw0uBDN5d2R_vqkSbGXqej4X2G7fGrGZ5ZEJAfdBgE130_head {
  this: np:hasAssertion dgn-np:NP266371.RArVw0uBDN5d2R_vqkSbGXqej4X2G7fGrGZ5ZEJAfdBgE130_assertion;
    np:hasProvenance dgn-np:NP266371.RArVw0uBDN5d2R_vqkSbGXqej4X2G7fGrGZ5ZEJAfdBgE130_provenance;
    np:hasPublicationInfo dgn-np:NP266371.RArVw0uBDN5d2R_vqkSbGXqej4X2G7fGrGZ5ZEJAfdBgE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP266371.RArVw0uBDN5d2R_vqkSbGXqej4X2G7fGrGZ5ZEJAfdBgE130_assertion a np:Assertion .
  
  dgn-np:NP266371.RArVw0uBDN5d2R_vqkSbGXqej4X2G7fGrGZ5ZEJAfdBgE130_provenance a np:Provenance .
  
  dgn-np:NP266371.RArVw0uBDN5d2R_vqkSbGXqej4X2G7fGrGZ5ZEJAfdBgE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP266371.RArVw0uBDN5d2R_vqkSbGXqej4X2G7fGrGZ5ZEJAfdBgE130_assertion {
  miriam-gene:81539 a ncit:C16612 .
  
  lld:C0032580 a ncit:C7057 .
  
  dgn-gda:DGNe520a64b93e23b2fcabee1d6c0d4f632 sio:SIO_000628 miriam-gene:81539, lld:C0032580;
    a sio:SIO_001121 .
}

dgn-np:NP266371.RArVw0uBDN5d2R_vqkSbGXqej4X2G7fGrGZ5ZEJAfdBgE130_provenance {
  dgn-np:NP266371.RArVw0uBDN5d2R_vqkSbGXqej4X2G7fGrGZ5ZEJAfdBgE130_assertion dcterms:description
      "[In this study, we determined the NAT2 genotype in members of one large FAP family and three smaller ones all of which had been shown to harbor the same germline APC gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:9156320;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP266371.RArVw0uBDN5d2R_vqkSbGXqej4X2G7fGrGZ5ZEJAfdBgE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}